Canonical Allele Identifier: CA2680487707
Gene: PEX7 HGNC NCBI

Linked Data

gnomAD v4: 6-136822501-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822501C>G , CM000668.2:g.136822501C>G GRCh38
NC_000006.11:g.137143639C>G , CM000668.1:g.137143639C>G GRCh37
NC_000006.10:g.137185332C>G NCBI36
NG_008462.1:g.4922C>G

Transcript Alleles

HGVS Amino-acid Change
XM_006715502.1:c.-165C>G XP_006715565.1:n.-165C>G
XM_011535900.1:c.-165C>G XP_011534202.1:n.-165C>G
XM_006715502.2:c.-165C>G XP_006715565.1:n.-165C>G
XM_017010934.2:c.-165C>G XP_016866423.1:n.-165C>G
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